Renal responses to acetazolamide and parethyroid hormone in carbonic anhydrase II. deficiency [PDF]
M Vainesel, F. Vertongen, William S. Sly
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Development of Human Carbonic Anhydrase II Heterobifunctional Degraders. [PDF]
O'Herin CB+5 more
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Carbonic Anhydrase II Deficiency in a Saudi Woman
Objective Carbonic anhydrase (CA) II deficiency is a rare autosomal recessive disorder caused by mutation in the CA II gene that leads to osteopetrosis, renal tubular acidosis (RTA), and cerebral calcification.
Omar N. Alhuzaim+2 more
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Some properties of site‐specific mutants of human carbonic anhydrase II having active‐site residues characterizing carbonic anhydrase III [PDF]
Xilin Ren+2 more
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In this study a series of pyrazole-3,4-dicarboxamide (3–10) derivatives bearing sulfonamide moiety were synthesized starting from 1-(3-nitrophenyl)-5-phenyl-1H-pyrazole-3,4-dicarboxylic acid (1). The structures of synthesized molecules were characterized
Samet Mert+5 more
doaj
Background: Carbonic anhydrase II (CA II) deficiency is a rare autosomal recessive genetic disorder presenting with the characteristic triad of osteopetrosis, renal tubular acidosis (RTA), and intracerebral calcifications.
Rajkumar Kundavaram+6 more
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High-activity carbonic anhydrase isoenzyme (CA II) in human gallbladder epithelium. [PDF]
Tatu Juvonen+7 more
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2-((1H-Benzo[d]imidazol-2-yl)amino)benzo[d]thiazole-6-sulphonamides: a class of carbonic anhydrase II and VII-selective inhibitors. [PDF]
Abdoli M, Supuran CT, Žalubovskis R.
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Biochemical and in silico inhibition of bovine and human carbonic anhydrase-II by 1H-1,2,3-triazole analogs. [PDF]
Khan M+6 more
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Immunoelectron microscopy of carbonic anhydrase isozyme VI in human submandibular gland: comparison with isozymes I and II. [PDF]
Y Ogawa+5 more
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